Finerenone

Modify Date: 2025-08-24 19:56:37

Finerenone Structure
Finerenone structure
Common Name Finerenone
CAS Number 1050477-31-0 Molecular Weight 378.42400
Density N/A Boiling Point N/A
Molecular Formula C21H22N4O3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Finerenone


Finerenone (BAY 94-8862) is a third-generation, selective, and orally available nonsteroidal mineralocorticoid receptor (MR) antagonist (IC50=18 nM). Finerenone displays excellent selectivity versus glucocorticoid receptor (GR), androgen receptor (AR), and progesterone receptor (>500-fold). Finerenone has the potential for cardiorenal diseases research, such as type 2 diabetes mellitus and chronic kidney disease[1][2].

 Names

Name (4S)-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,4-dihydro-1,6-naphthyridine-3-carboxamide
Synonym More Synonyms

 Finerenone Biological Activity

Description Finerenone (BAY 94-8862) is a third-generation, selective, and orally available nonsteroidal mineralocorticoid receptor (MR) antagonist (IC50=18 nM). Finerenone displays excellent selectivity versus glucocorticoid receptor (GR), androgen receptor (AR), and progesterone receptor (>500-fold). Finerenone has the potential for cardiorenal diseases research, such as type 2 diabetes mellitus and chronic kidney disease[1][2].
Related Catalog
In Vivo Finerenone (BAY 94-8862) lowers albuminuria by >40% and significantly reduces systolic blood pressure (SBP) in Munich Wistar Frömter (MWF) rat[1]. Animal Model: Twelve-week-old MWF rat[1] Dosage: 10 mg/kg Administration: P.o.; daily for 4 weeks Result: Significantly reduced SBP in MWF rats; led to a significant reduction (>40%) in albuminuria in the MWF model. Animal Model: Twelve-week-old MWF rat[1] Dosage: 10 mg/kg Administration: P.o.; daily for 4 weeks Result: Significantly reduced SBP in MWF rats; led to a significant reduction (>40%) in albuminuria in the MWF model.
References

[1]. Bärfacker L, et al. Discovery of BAY 94-8862: a nonsteroidal antagonist of the mineralocorticoid receptor for the treatment of cardiorenal diseases. ChemMedChem. 2012;7(8):1385-1403.

[2]. González-Blázquez R, et al. Finerenone Attenuates Endothelial Dysfunction and Albuminuria in a Chronic Kidney Disease Model by a Reduction in Oxidative Stress. Front Pharmacol. 2018;9:1131. Published 2018 Oct 9.

 Chemical & Physical Properties

Molecular Formula C21H22N4O3
Molecular Weight 378.42400
Exact Mass 378.16900
PSA 111.25000
LogP 4.27338

 Safety Information

Hazard Codes T+

 FinerenoneBioassay

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Name: Human Mineralocorticoid receptor (3C. 3-Ketosteroid receptors)
Source: IUPHAR-DB
Target: Mineralocorticoid receptor (3C. 3-Ketosteroid receptors) [Homo sapiens]
External Id: 626_Human
Name: ASTRAZENECA: Octan-1-ol/water (pH7.4) distribution coefficent measured by a shake fl...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301363
Name: ASTRAZENECA: Most basic pKa value (pKa B1) determined by absorption and potentiometri...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301362
Name: ASTRAZENECA: % bound to plasma by equilibrium dialysis. Compound is incubated with wh...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301365
Name: ASTRAZENECA: % bound to plasma by equilibrium dialysis. Compound is incubated with wh...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301366
Name: Induction of improvement in urinary albumin-creatinine ratio in patient with diabetic...
Source: ChEMBL
Target: Homo sapiens
External Id: CHEMBL4008047
Name: ASTRAZENECA: % bound to plasma by equilibrium dialysis. Compound is incubated with wh...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301368
Name: ASTRAZENECA: Intrinsic clearance measured in rat hepatocytes following incubation at ...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301371
Name: Ratio of IC50 for Gal4-fused human MR Ser810 mutant expressed in HEK293T cells to IC5...
Source: ChEMBL
Target: N/A
External Id: CHEMBL4008017
Name: ASTRAZENECA: Intrinsic clearance measured in human liver microsomes following incubat...
Source: ChEMBL
Target: N/A
External Id: CHEMBL3301370
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 Synonyms

Finerenone
UNII-DE2O63YV8R
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